Quality Control for Microbiological Media and Reagents

Duration: 60 Minutes
This 1-hour virtual seminar will give you the tools you need to maintain a quality supply of media and reagents in a variety of microbiology laboratories. A thorough understanding of variety of challenges is necessary to maintain quality of the media and reagents will be brought to the fore. This will allow you to perform microbiology testing with confidence.
Microbiological Media and Reagents
Instructor: Todd Graham
Product ID: 501036

Why Should you Attend
In microbiology laboratories, there are a wide array and media for all sorts of use. From clinical laboratories, to environmental monitoring, from research laboratories to industrial labs, there are a large number of different set-ups. These media and reagents need to be monitored on a regular basis to ensure that the work performed in these laboratories is accurate and true. Otherwise, false results will be reported, which can lead to serious consequences and harm the public health in a myriad of ways.

This webinar will cover a variety of different media and reagents, and will discuss the quality control methods. This will allow your laboratory to develop the plan that is right for your needs and help you succeed in meeting the laboratory's goals.

Objectives of the Presentation
This webinar will help you develop a quality control program that fits your microbiological laboratory's needs. We will explicitly not cover any serological, immunological or molecular tests. The webinar will include the critical information like:
  • Why quality control for these reagents?
  • Quality control for solid media
  • Quality control for liquid media
  • Quality control for media kits
  • Quality control for biochemical reagents
  • How to integrate quality control for various media and reagents
Who can Benefit
This topic applies to personnel / companies any industry that requires regular microbiology testing as a part of their business.
  • Senior Management
  • Quality Assurance
  • Research and Development
  • Facilities Staff
$375
Recorded Session for one participant
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  $500.00 Training CD
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  $600.00 Flash Drive
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How it works
Live Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • The webinar joining link, username and password for joining the webinar will be updated on your OCP Account 24 hours prior to the webinar
  • Presentation handouts in Downloadable PDF format will be updated on your OCP Account 24 hours prior to the live session
  • Login to the audio conference on the scheduled date and time
  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Todd Graham is a masters-level bench scientist and medical technologist with a host of experience in both clinical diagnostics and biotechnology fields. He has worked for a number of start-up firms in the clinical diagnostics and biotechnology industries, as well as worked for larger firms within both industries. He has a broad level of expertise in assay development for quality control, pharmaceutical development and clinical diagnostics. His particular levels of expertise are in molecular diagnostics, PCR, ELISA, quality control and training of bench level personnel in clinical diagnostics and biotechnology. He has established a consultancy to assists academic labs in transitioning their research to industry by verifying and improving the quality of their work.


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